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4-Chloro-3-(N-Morpholinecarbonyl)Phenylboronic Acid is an organic compound that features a boronic acid group attached to a chlorophenyl ring with a morpholinecarbonyl substituent. This unique structure endows it with versatile reactivity and functional group compatibility, making it a valuable intermediate in organic synthesis and a key component in various chemical reactions.

871332-71-7

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871332-71-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-3-(N-Morpholinecarbonyl)Phenylboronic Acid is used as a synthetic intermediate for the development of pharmaceutical compounds. Its ability to participate in the Suzuki-Miyaura coupling reaction allows for the formation of new carbon-carbon bonds, which is crucial for constructing complex molecular frameworks and creating novel drug candidates with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, 4-Chloro-3-(N-Morpholinecarbonyl)Phenylboronic Acid is utilized as a reagent in various organic reactions. Its involvement in the Suzuki-Miyaura coupling reaction is particularly noteworthy, as it enables the synthesis of a wide range of biaryl compounds, which are prevalent in pharmaceuticals, agrochemicals, and materials science.
Used in Material Science:
4-Chloro-3-(N-Morpholinecarbonyl)Phenylboronic Acid is employed as a building block in the synthesis of advanced materials. The Suzuki-Miyaura coupling reaction, in which 4-CHLORO-3-(N-MORPHOLINECARBONYL)PHENYLBORONIC ACID participates, allows for the creation of new materials with tailored properties, such as improved conductivity, stability, or specific interactions with other molecules, which can be applied in various high-tech industries.
Overall, 4-Chloro-3-(N-Morpholinecarbonyl)Phenylboronic Acid is a versatile and valuable chemical entity with applications spanning across the pharmaceutical, chemical research, and material science industries. Its role in the Suzuki-Miyaura coupling reaction highlights its potential in the synthesis of complex and functional molecules, contributing to the advancement of these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 871332-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,3,3 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 871332-71:
(8*8)+(7*7)+(6*1)+(5*3)+(4*3)+(3*2)+(2*7)+(1*1)=167
167 % 10 = 7
So 871332-71-7 is a valid CAS Registry Number.

871332-71-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H53336)  4-Chloro-3-(4-morpholinylcarbonyl)benzeneboronic acid, 98%   

  • 871332-71-7

  • 250mg

  • 1158.0CNY

  • Detail
  • Alfa Aesar

  • (H53336)  4-Chloro-3-(4-morpholinylcarbonyl)benzeneboronic acid, 98%   

  • 871332-71-7

  • 1g

  • 3704.0CNY

  • Detail

871332-71-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Chloro-3-(morpholine-4-carbonyl)phenyl)boronic acid

1.2 Other means of identification

Product number -
Other names [4-chloro-3-(morpholine-4-carbonyl)phenyl]boronic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:871332-71-7 SDS

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